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Neoplasia  223

            with peripheral or nonuniform contrast enhancement.    hemorrhage.  Ependymomas may be accommodated
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                                                                         4,5
            Tumor‐related  production of  vascular permeability   by gradual ventricular dilation, hence edema is usually
              factors, such as vascular endothelial growth factor, may   absent or minimal, unless the tumor invades the perive­
            also contribute to contrast enhancement in high‐grade   ntricular brain parenchyma or hydrocephalus causes
            gliomas. 6                                         periventricular interstitial edema.
               The appearance of oligodendrogliomas on unen­     Ependymomas are typically isoattenuating on
            hanced  CT  images  is  similar to that  of  astrocytomas.     unenhanced CT images, although they can have a
            They are typically hypoattenuating, and mass margins     heterogeneous appearance.
            may be ill defined or lacking, particularly when     Ependymomas appear slightly T1 hypointense to
              peritumoral edema is present. Marked central hypoat­  slightly hyperintense on unenhanced images and mod­
            tenuation of some oligodendrogliomas, caused by the   erately to markedly T2 hyperintense.
            high water content of the mucinous core, may increase   Contrast enhancement is usually marked and may be
            the index of suspicion for this tumor.             heterogeneous, which reflects the coarse texture of the
               Oligodendrogliomas are moderately T1 hypointense   tumor parenchyma, on both CT and MR images. 27,30,31
            and markedly T2 hyperintense, specifically when there is   Heterogeneity may be even more pronounced when
            significant central mucinous content. Peritumoral edema   cysts or hemorrhage are present. Tumor margins are
            ranges from minimal to moderate, although even large   typically distinct, because the majority of the mass
            oligodendrogliomas may induce little edema formation.  extends into a ventricular lumen (Figure 2.8.13).
               Contrast enhancement of oligodendrogliomas on both
            CT and MR images is highly variable, ranging from none   Choroid plexus tumors
            to marked, and when present it is often peripheral or non­  Choroid plexus tumors (CPT) are relatively common
            uniform. Focal or regional contrast enhancement is often   neoplasms that arise from the choroid plexus epithelium
            distributed centrally or eccentrically within the greater   within the lateral, third, and fourth ventricles and the lat­
            tumor volume  and  may  have  a  serpentine  shape. 21,27–29    eral recesses. About 50% originate in the fourth  ventricle
            Although high‐grade oligodendrogliomas tend to con­  or lateral recesses. The average age of dogs at diagnosis is
            trast enhance to a greater degree than low‐grade tumors,   6 years, which is earlier than most other intracranial
            as with astrocytoma, this imaging feature is not a reliable   tumors. Golden Retrievers appear to be highly overrep­
            indicator of biological grade (Figure 2.8.11, 2.8.12).  resented.  Classification of canine CPT distinguishes
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                                                               choroid plexus papillomas (CPP), comparable to WHO
            Mixed glial cell tumors                            grade I and morphologically benign, from choroid
            Canine mixed glial tumors are usually comprised of   plexus carcinomas (CPC), comparable to WHO grade
                                                               III  and histologically  more abnormal and  more likely
            tumor cells with both astrocytic and oligodendrocytic   to  invade the brain or give rise to intraventricular
            features, or they may contain a combination of astrocytic   or intrathecal metastases.  Mild to moderate edema is
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            and  oligodendrocytic  subpopulations.  These  tumors     present in about 45% of CPP and about 70% of CPC. 32
            have MR imaging features similar to those of astrocyto­  Choroid plexus tumors share many CT and MR
            mas and oligodendrogliomas.
                                                                 imaging features with ependymomas. Initially, they may
                                                               conform to the shape of the ventricle in which they grow,
            Ependymal tumors                                   but enlargement may lead to hydrocephalus because of
            Ependymomas are uncommon tumors that arise from    ventricular obstruction or, possibly, overproduction of
            the ependymal lining cells of the ventricular system and   CSF. Tumors have variable attenuation on unenhanced
            thus  may  occur  within  the  ventricular  system of  the   CT images and may be T1 hypo‐, iso‐, or hyperintense
            brain and spinal cord. Ependymomas usually affect   and T2 hyperintense on MR images. Choroid plexus
            older dogs and cats without breed predisposition. These   tumors often appear heterogeneous, particularly when
            tumors are predominantly intraventricular, although   there is intratumoral hemorrhage.
            some invade the adjacent brain parenchyma, and they   Choroid plexus tumors usually show marked, uniform
            expand to fill the ventricular cavity in which they arise,   enhancement on  both CT  and MR  images  following
            causing distortion of the ventricle and obstructive   contrast administration, which reflects the underlying
            hydrocephalus, depending on their size and location.   papillary vascular architecture of these tumors
            Ependymomas may be well differentiated (WHO grade   (Figure  2.8.14). Intraventricular and intrathecal “drop
            II) or anaplastic and aggressive (WHO grade III).   metastases” may appear as intensely contrast‐enhancing
            Grossly, the tumors can be soft, lobular (papillary type),   foci in the ventricles or subarachnoid space
            or solid (cellular subtype) and may contain cysts and/or   (Figure  2.8.15). Choroid plexus papillomas and

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